Preparation and characterization of thermoresponsive poly(N-isopropylacrylamide) copolymers with enhanced hydrophilicity

The poly(N-isopropylacrylamide) copolymers with the enhanced hydrophilicity were synthesized by free radical polymerization from a mixture of the monomers N-isopropylacrylamide (NIPAAm), N-vinyl pyrrolidone (NVP), hydroxypropyl methacrylate (HPM) and 3-trimethoxysilypropyl methacrylate (TMSPM) at different feeding ratios. The attenuated total reflectance-Fourier transform infrared spectrometry (ATR-FTIR), nuclear magnetic resonance (H-1-NMR) and gel permeation chromatography (GPC) were applied to characterize the resultant copolymers. The lower critical solution temperature (LCST) of the copolymers was determined via dynamic light scattering (DLS). By alternating the molar ratios of NIPAAm and NVP, the copolymers were synthesized to have their own distinctive LCST from 25 degrees C to 40 degrees C. Regardless of the starting feed ratio used, the final copolymers had the similar monomeric ratio as planned. The copolymer films were then formed on platinum wafers by drop coating and thermal annealing owing to 3-trimethoxysilyl crosslinking and reacting with hydroxyl groups. The surface wettability and morphology of the specimens were observed using contact angle measurements and scanning electron microscopy (SEM), respectively. The results demonstrated that with the increase of the NVP content, the film surface became more hydrophilic. The surface microstructure of the thermoresponsive films varied depending on the copolymer composition and ambient temperature. The experimental results indicated that the addition of NVP not only increased the LCST of copolymers but also improved the hydrophilicity of the products derived from the copolymers. This ability to elevate the LCST of the polymers provides excellent flexibility in tailoring transitions for specific uses, like controlled drug release and nondestructive cell harvest.